Demo Data from SIGIR 2026 / reviewers in the wild / expert
Bianca Haase
dblp:158/8454
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2015
0000-0001-6493-9808ORCID · reported
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › genomics
genotyping |
0.2 | 1 | 2015 | Simple, rapid and accurate genotyping-by-sequencing from aligned whole genomes with ArrayMaker · Bioinform. 2015 |
Bioinformatics and computational biology › genomics › genotyping
genotyping-by-sequencing |
0.2 | 1 | 2015 | Simple, rapid and accurate genotyping-by-sequencing from aligned whole genomes with ArrayMaker · Bioinform. 2015 |
Bioinformatics and computational biology › genomics
genome-wide association study |
0.1 | 1 | 2015 | Simple, rapid and accurate genotyping-by-sequencing from aligned whole genomes with ArrayMaker · Bioinform. 2015 |
Methods — techniques the papers use, named apart from their topics
whole-genome alignment · 0.2
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2015 | Simple, rapid and accurate genotyping-by-sequencing from aligned whole genomes with ArrayMakerabstractSUMMARY: Whole-genome sequencing has revolutionized the study of genetics. Genotyping-by-sequencing is now a viable method of genotyping, yet the bioinformatics involved can be daunting if not prohibitive for some laboratories. Here we present ArrayMaker, a user-friendly tool that extracts accurate single nucleotide polymorphism genotypes at pre-defined loci from whole-genome alignments and presents them in a standard genotyping format compatible with association analysis software and datasets genotyped on commercial array platforms. Using this tool, geneticists with only basic computing ability can genotype samples at any desired list of markers, facilitating genome-wide association analysis, fine mapping, candidate variant assessment, data sharing and compatibility of data sourced from multiple technologies. AVAILABILITY AND IMPLEMENTATION: ArrayMaker is licensed under The MIT License and can be freely obtained at https://github.com/cw2014/ArrayMaker/. The program is implemented in Perl and runs on Linux operating systems. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. CONTACT: [email protected]. Cali E. Willet, Bianca Haase, Michael A. Charleston, Claire M. Wade |
Bioinform. | 2 |